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Analysis of the Specificity and Persistence of Nasal Immune Responses to Respiratory Viral Antigens in Immunocompromised and Healthy Cohorts

Analysis of the Specificity and Persistence of Nasal Immune Responses to Respiratory Viral Antigens in Immunocompromised and Healthy Cohorts

Recruiting
18-90 years
All
Phase N/A

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Overview

The goal of this observational study is to characterize nasal mucosal immunity to respiratory viruses, such as SARS-CoV-2, in immunocompromised individuals and healthy volunteers.

The study involves adults of any sex, between 18 and 90 years old, including both immunocompromised patients with medical conditions or treatments that can affect immune cell functions and healthy controls with no underlying medical conditions declared, no clinical history of immunodeficiency or use of immunosuppressive medications.

Researchers will compare immunocompromised participants to healthy volunteers to determine how underlying immunodeficiency and related treatments affect immune cell composition and virus-specific responses.

Eligibility

Inclusion Criteria:

  • Informed Consent: Participants must have signed an informed consent form.
  • Age Range: Participants aged between 18 and 90 years.
  • Healthy Immunocompetent Donors: no underlying medical conditions declared, no clinical history of immunodeficiency or use of immunosuppressive medications.
  • Immunocompromised Patients: subjects with medical conditions or treatments associated with significant impairment of the immune system. This may include organ or stem cell transplants, ongoing immunosuppressive therapies, documented genetic immunosuppression.

Exclusion Criteria:

  • Pregnant or lactating women.
  • Individuals unable to provide informed consent

Study details
    Immuno-modulation
    Immuno-suppression
    Immunocompromised Patients
    Healthy Subjects
    Oncological Patients

NCT07295535

Fondazione IRCCS Policlinico San Matteo di Pavia

31 January 2026

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